Wiskott-Aldrich syndrome

A primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies.

Hemolytic anemia

A type of anemia caused by premature destruction of red blood cells (hemolysis).


Total: 1

                      


(per page)
PMID (PMCID)
7749101
MIXED_SAMPLE Infant, Newborn
Umbilical cord blood infusion in a patient for correction of Wiskott-Aldrich syndrome.
Kernan NA, Schroeder ML, Ciavarella D, Preti RA, Rubinstein P, O'Reilly RJ.
Blood Cells. 1994;20(2-3):245-8.
A 2 3/4 year old male with thrombocytopenia secondary to Wiskott-Aldrich Syndrome (WAS) and a history of two intracranial hemorrhages as well as hemolytic anemia and neutropenia received a placental blood infusion from an HLA-identical female sibling born by caesarian section at 35 weeks gestation.